Assessment of bone metastases in patients (pts) with urothelial carcinoma using 18 F-sodium fluoride PET/CT ( 18 F-NaF) versus 18 F-fluorodeoxyglucose PET/CT ( 18 F-FDG)

Abstract only 329 Background: 18 F-NaF has shown improved sensitivity for bone imaging when compared to conventional planar imaging or SPECT/CT using 99m Tc-MDP. We compared the number of bone lesions detected on 18 F-NaF versus 18 F-FDG in urothelial cancer pts with known bone metastases undergoing...

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Published inJournal of clinical oncology Vol. 32; no. 4_suppl; p. 329
Main Authors Weinberg, Benjamin Adam, Lindenberg, Maria Liza, Kurdziel, Karen A., Steinberg, Seth M., Liewehr, David J., Khadar, Kattie, McKinney, Yolanda, Choyke, Peter L., Apolo, Andrea Borghese
Format Journal Article
LanguageEnglish
Published 01.02.2014
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Summary:Abstract only 329 Background: 18 F-NaF has shown improved sensitivity for bone imaging when compared to conventional planar imaging or SPECT/CT using 99m Tc-MDP. We compared the number of bone lesions detected on 18 F-NaF versus 18 F-FDG in urothelial cancer pts with known bone metastases undergoing treatment. Methods: Pts enrolled in a prospective single-arm phase II study of cabozantinib underwent 18 F-NaF and 18 F-FDG scans at baseline and at 8 weeks of therapy. In a lesion-based analysis independently confirmed by a nuclear medicine physician, abnormal foci of radiotracer uptake were categorized by location (skull, spine, pelvis, thorax, or long bones) and by disease state (benign, malignant, or indeterminate). A patient-based analysis was performed to determine if findings indicated disease progression, stable disease, or improvement of disease, based on the number of lesions and standardized uptake values (SUVs). Results: 294 total bone lesions were identified at baseline in 10 pts (8 male and 2 female, ages 44-73). 18 F-NaF identified more lesions than 18 F-FDG at baseline, 294 vs. 119. In a paired analysis, the median difference was 11.5 more lesions detected per patient on 18 F-NaF vs. 18 F-FDG (by Wilcoxon signed-rank test, p = 0.023). More total thoracic bone lesions at baseline, 100 vs. 23, were also detected on 18 F-NaF vs. 18 F-FDG, median 6.5 vs. 1.0 with a median difference of 6 more lesions per patient on 18 F-NaF (p = 0.016). 18 F-NaF also detected more skull lesions at baseline, 19 vs. 1, which was clinically but not statistically significant (p = 0.250). There was general concordance in the patient-based analysis; only 1 18 F-NaF scan demonstrated progressive disease while its corresponding 18 F-FDG scan showed stable disease. Conclusions: 18 F-NaF identified more lesions than 18 F-FDG at baseline, making it a good staging exam. However, there was agreement between 18 F-NaF and 18 F-FDG in terms of tumor response in almost all the follow-up scans. Therefore, although a greater number of bone lesions are seen in 18 F-NaF compared with 18 F-FDG, the clinical significance in assessing treatment response remains to be determined. Clinical trial information: NCT01688999.
ISSN:0732-183X
1527-7755
DOI:10.1200/jco.2014.32.4_suppl.329